Obasi Avemaria, Nwachukwu SimonCyril, Ugoji Esther, Kohler Christian, Göhler André, Balau Veronica, Pfeifer Yvonne, Steinmetz Ivo
1 Department of Microbiology, University of Lagos , Lagos, Nigeria .
2 Department of Medical Microbiology, Friedrich Loeffler Institute for Medical Microbiology, University of Greifswald , Greifswald, Germany .
Microb Drug Resist. 2017 Dec;23(8):1013-1018. doi: 10.1089/mdr.2016.0269. Epub 2017 Apr 4.
Emergence and spread of Klebsiella pneumoniae isolates producing extended-spectrum β-lactamases (ESBLs) present a major threat to public health. In this study, we characterized β-lactam-resistant K. pneumoniae isolates from six wastewater samples obtained from two pharmaceutical industries located in Lagos and Ogun States, Nigeria. Bacteria were isolated by using MacConkey agar; species identification and antibacterial susceptibility testing were performed by Vitek 2. Etest was used for ESBL phenotype confirmation. The presence of β-lactamase genes was investigated by PCR and sequencing. Bacterial strain typing was done by XbaI-macrorestriction and subsequent pulsed-field gel electrophoresis (PFGE) as well as multilocus sequence typing (MLST). Thirty-five bacterial species were isolated from the six samples; among them, we identified seven K. pneumoniae isolates with resistance to β-lactams and co-resistance to fluoroquinolones, aminoglycosides, and folate pathway inhibitors. The ESBL phenotype was confirmed in six K. pneumoniae isolates that harbored ESBL genes bla (n = 5), bla (n = 1), and bla (n = 1). PFGE and MLST analysis revealed five clones belonging to four sequence types (ST11, ST15, ST37, ST101), and clone K. pneumoniae-ST101 was present in the wastewater samples from two different pharmaceutical industries. Additionally performed conjugation assays confirmed the location of β-lactamase genes on conjugative plasmids. This is the first confirmation of K. pneumoniae isolates producing CTX-M-15-ESBL from pharmaceutical wastewaters in Nigeria. The co-resistance observed might be a reflection of the different drugs produced by these industries. Continuous surveillance of the environmental reservoirs of multidrug-resistant bacteria is necessary to prevent their further spread.
产超广谱β-内酰胺酶(ESBLs)的肺炎克雷伯菌分离株的出现和传播对公众健康构成了重大威胁。在本研究中,我们对从尼日利亚拉各斯和奥贡州的两家制药厂采集的六个废水样本中的耐β-内酰胺肺炎克雷伯菌分离株进行了特征分析。使用麦康凯琼脂分离细菌;通过Vitek 2进行菌种鉴定和抗菌药敏试验。采用Etest确认ESBL表型。通过PCR和测序研究β-内酰胺酶基因的存在情况。通过XbaI宏限制性内切酶消化及随后的脉冲场凝胶电泳(PFGE)以及多位点序列分型(MLST)进行细菌菌株分型。从六个样本中分离出35种细菌;其中,我们鉴定出七株对β-内酰胺类耐药且对氟喹诺酮类、氨基糖苷类和叶酸途径抑制剂具有共耐药性的肺炎克雷伯菌分离株。在六株携带ESBL基因bla(n = 5)、bla(n = 1)和bla(n = 1)的肺炎克雷伯菌分离株中确认了ESBL表型。PFGE和MLST分析揭示了属于四种序列类型(ST11、ST15、ST37、ST101)的五个克隆,并且肺炎克雷伯菌-ST101克隆存在于来自两家不同制药厂的废水样本中。另外进行的接合试验证实了β-内酰胺酶基因位于接合质粒上。这是尼日利亚首次从制药废水中确认产CTX-M-15-ESBL的肺炎克雷伯菌分离株。观察到的共耐药性可能反映了这些工厂生产的不同药物。持续监测多重耐药菌的环境储存库对于防止其进一步传播是必要的。